A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3370



Internal ID15547973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37578286..37611702hg38UCSC Ensembl
Outerchr20:36206688..36240104hg19UCSC Ensembl
Outerchr20:35640102..35673518hg18UCSC Ensembl
Outerchr20:35640102..35673518hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg387580
hg197580
hg187580
hg177580
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1602
SamplesNA19240
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv3370
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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